Manilkara hexandra

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Synonyms

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Subtypes (subspecies, varieties, subvarieties, forms)

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Scientific Literature

Phytochemical Profile

Biological Material

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Details Top

Internal ID	UUID643fe2984d123410323201
Scientific name	Manilkara hexandra
Authority	Dubard
First published in	Ann. Mus. Colon. Marseille , sér. 3, 3: 9 (1915)

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Synonyms Top

Scientific name	Authority	First published in
Kaukenia hexandra	Kuntze	Revis. Gen. Pl. 2: 406 (1891)
Manilkara emarginata	H.J.Lam	Bull. Jard. Bot. Buitenzorg , sér. 3, 7: 241 (1925)
Mimusops hexandra	Roxb.	Pl. Coromandel 1: 16 (1795)
Mimusops indica	A.DC.	Prodr. 8: 205 (1844)

Common names Top

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Filter by language:

Language	Common/alternative name
Bengali	খিরনি
Persian	خیز نی
Gujarati	રાયણ
Hindi	खिरनी
Malayalam	പഴമൂൺപാല
Marathi	खिरणी
sd	کيرڻي(وڻ)
Tamil	பாலை
Telugu	మనిల్కరా హెక్సాండ్ర
Telugu	పాలపండ్లు
Thai	เกด
Chinese	铁色
Chinese	铁线子

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - China Southeast
  - Hainan

Asia-tropical click to expand
- Indian Subcontinent
  - Bangladesh
  - India
  - Sri Lanka
- Indo-China
  - Cambodia
  - Myanmar
  - Thailand
  - Vietnam
- Malesia
  - Malaya

Links to other databases Top

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Database	ID/link to page
World Flora Online	wfo-0000235885
Tropicos	28701423
KEW	urn:lsid:ipni.org:names:787644-1
The Plant List	kew-120170
Open Tree Of Life	603207
NCBI Taxonomy	233706
IPNI	787644-1
iNaturalist	541885
GBIF	2885079
Freebase	/m/05f83_c
EOL	1154599
USDA GRIN	102661
Wikipedia	Manilkara_hexandra

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.

Title

Authors

Publication

Released

IDs

Separation Methods of Phenolic Compounds from Plant Extract as Antioxidant Agents Candidate

Susanti I, Pratiwi R, Rosandi Y, Hasanah AN

Plants (Basel)

27-Mar-2024

PMCID:	PMC11013868
doi:	10.3390/plants13070965
PMID:	38611494

An Alarming Decline in the Nutritional Quality of Foods: The Biggest Challenge for Future Generations’ Health

Bhardwaj RL, Parashar A, Parewa HP, Vyas L

Foods

14-Mar-2024

PMCID:	PMC10969708
doi:	10.3390/foods13060877
PMID:	38540869

Silvicultural Practices for Diversity Conservation and Invasive Species Suppression in Forest Ecosystems of the Bundala National Park, Sri Lanka

Suraweera C, Gallo J, Vacek Z, Cukor J, Vacek S, Baláš M

Plants (Basel)

31-Dec-2023

PMCID:	PMC10780521
doi:	10.3390/plants13010121
PMID:	38202429

Wood decay fungi show enhanced biodeterioration of low-density polyethylene in the absence of wood in culture media

Perera P, Herath H, Paranagama PA, Wijesinghe P, Attanayake RN

PLoS One

26-Jul-2023

PMCID:	PMC10370761
doi:	10.1371/journal.pone.0288133
PMID:	37494333

Mapping of traditional healthcare providers and their healing approaches in a tribal community of district Sirohi, Rajasthan

Dwivedi R, Goyal P, Yadav SS, Dwivedi P, Singh P, Singh K

J Family Med Prim Care

30-Jun-2023

PMCID:	PMC10451593
doi:	10.4103/jfmpc.jfmpc_1610_22
PMID:	37636156

A multivariate and quantitative assessment of medicinal plants used by the indigenous Malayali tribes in the Javadhu hills of Tiruvannamalai district, Tamil Nadu, India

Silambarasan R, Sasidharan S, Nair J H, Kumar S N, R A, Nair AS, Selavinayagam KT

Heliyon

18-Apr-2023

PMCID:	PMC10256831
doi:	10.1016/j.heliyon.2023.e15607
PMID:	37305490

Inventorization and Consensus Analysis of Ethnoveterinary Medicinal Knowledge Among the Local People in Eastern India: Perception, Cultural Significance, and Resilience

Mandal SK, Rahaman CH

Front Pharmacol

29-Apr-2022

PMCID:	PMC9099233
doi:	10.3389/fphar.2022.861577
PMID:	35571138

Inhibition of the main protease of SARS-CoV-2 (Mpro) by repurposing/designing drug-like substances and utilizing nature’s toolbox of bioactive compounds

Antonopoulou I, Sapountzaki E, Rova U, Christakopoulos P

Comput Struct Biotechnol J

14-Mar-2022

PMCID:	PMC8920478
doi:	10.1016/j.csbj.2022.03.009
PMID:	35308802

An overview of potential inhibitors targeting non-structural proteins 3 (PLpro and Mac1) and 5 (3CLpro/Mpro) of SARS-CoV-2

Yan F, Gao F

Comput Struct Biotechnol J

24-Aug-2021

PMCID:	PMC8382591
doi:	10.1016/j.csbj.2021.08.036
PMID:	34457214

DNA barcoding identifies cryptic animal tool materials

Steele MP, Neaves LE, Klump BC, St Clair JJ, Fernandes JR, Hequet V, Shaw P, Hollingsworth PM, Rutz C

Proc Natl Acad Sci U S A

12-Jul-2021

PMCID:	PMC8307691
doi:	10.1073/pnas.2020699118
PMID:	34253607

Impacts of community forestry on forest condition: Evidence from Sri Lanka’s intermediate zone

Ekanayake EM, Cirella GT, Xie Y

PLoS One

30-Sep-2020

PMCID:	PMC7526917
doi:	10.1371/journal.pone.0239405
PMID:	32997680

Inhibition of SARS-CoV-2 main protease by phenolic compounds from Manilkara hexandra (Roxb.) Dubard assisted by metabolite profiling and in silico virtual screening

Abd El-Mordy FM, El-Hamouly MM, Ibrahim MT, El-Rheem GA, Aly OM, Abd El-kader AM, Youssif KA, Abdelmohsen UR

RSC Adv

28-Aug-2020

PMCID:	PMC9056568
doi:	10.1039/d0ra05679k
PMID:	35518160

Pathogen and host genetics underpinning cryptococcal disease

Coelho C, Farrer RA

Adv Genet

18-Mar-2020

PMCID:	PMC7612911
doi:	10.1016/bs.adgen.2020.02.001
PMID:	32560785

Morphological and molecular barcode analysis of the medicinal tree Mimusops coriacea (A.DC.) Miq. collected in Ecuador

Bustamante K, Santos-Ordóñez E, Miranda M, Pacheco R, Gutiérrez Y, Scull R

PeerJ

11-Oct-2019

PMCID:	PMC6791349
doi:	10.7717/peerj.7789
PMID:	31616590

Consumption patterns of wild edibles by the Vasavas: a case study from Gujarat, India

Chauhan SH, Yadav S, Takahashi T, Łuczaj Ł, D’Cruz L, Okada K

J Ethnobiol Ethnomed

29-Aug-2018

PMCID:	PMC6116503
doi:	10.1186/s13002-018-0254-3
PMID:	30157859

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Benzenoids / Phenols / Benzenediols / Catechols
(4aS,8aS)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-4a,8a-dihydrochromen-4-one	162995241	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3C(O2)C=C(C=C3O)O)O)O)O	304.25	unknown	https://doi.org/10.1016/S0031-9422(00)85821-5 https://doi.org/10.1016/S0031-9422(00)82170-6
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
[1,3-Diacetyloxy-5-hydroxy-7,8-dimethyl-7-(3-methylidenepent-4-enyl)-1,3,5,6,6a,8,9,10-octahydrobenzo[d][2]benzofuran-10-yl] deca-2,4-dienoate	162891209	Click to see CCCCCC=CC=CC(=O)OC1CC(C(C2C13C(OC(C3=CC(C2)O)OC(=O)C)OC(=O)C)(C)CCC(=C)C=C)C	584.70	unknown	https://doi.org/10.1016/S0031-9422(00)85821-5 https://doi.org/10.1016/S0031-9422(00)86183-X
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
(4,4,6a,6a,8a,11,11,14b-Octamethyl-1,2,3,4a,5,6,8,9,10,12,12a,13,14,14a-tetradecahydropicen-3-yl) acetate	5205968	Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CCC4(C3=CCC5(C4CC(CC5)(C)C)C)C)C)C	468.80	unknown	https://doi.org/10.1016/S0031-9422(00)82170-6 https://doi.org/10.1016/S0031-9422(00)85821-5
[(3S,4aS,6aR,6aR,8aR,12aS,14aS,14bR)-4,4,6a,6a,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,8,9,10,12,12a,13,14,14a-tetradecahydropicen-3-yl] acetate	162948602	Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CCC4(C3=CCC5(C4CC(CC5)(C)C)C)C)C)C	468.80	unknown	https://doi.org/10.1016/S0031-9422(00)82170-6 https://doi.org/10.1016/S0031-9422(00)85821-5
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
6-[[8a-[3-[5-[3,5-Dihydroxy-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-3,4-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxycarbonyl-2,5,8-trihydroxy-4-(hydroxymethyl)-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid	74203438	Click to see CC1C(C(C(C(O1)OC2C(COC(C2O)OC3C(OC(C(C3O)O)OC4C(C(COC4OC(=O)C56CCC(CC5C7=CCC8C9(CC(C(C(C9C(CC8(C7(CC6O)C)C)O)(C)CO)OC1C(C(C(C(O1)C(=O)O)O)O)O)O)C)(C)C)O)O)C)O)O)O)O	1253.30	unknown	https://doi.org/10.1016/0031-9422(95)00692-3
Tieghemelin	11051494	Click to see CC1C(C(C(C(O1)OC2C(COC(C2O)OC3C(OC(C(C3O)O)OC4C(C(COC4OC(=O)C56CCC(CC5C7=CCC8C9(CC(C(C(C9C(CC8(C7(CC6O)C)C)O)(C)CO)OC1C(C(C(C(O1)C(=O)O)O)O)O)O)C)(C)C)O)O)C)O)O)O)O	1253.30	unknown	https://doi.org/10.1016/0031-9422(95)00692-3
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,4aS,6aR,6bS,8aR,11R,12S,12aS,14aR,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol	163022461	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C	426.70	unknown	https://doi.org/10.1016/S0031-9422(00)86183-X https://doi.org/10.1016/S0031-9422(00)85821-5
(4,4,6a,6b,8a,11,11,14b-Octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl) 3-phenylprop-2-enoate	612772	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C=CC6=CC=CC=C6)C)C)C2C1)C)C)C	556.90	unknown	https://doi.org/10.1016/S0031-9422(00)85673-3
[(3S,4aR,6aR,6bS,8aR,12aS,14aR,14bS)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] (E)-3-phenylprop-2-enoate	163195568	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C=CC6=CC=CC=C6)C)C)C2C1)C)C)C	556.90	unknown	https://doi.org/10.1016/S0031-9422(00)85673-3
4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol	225688	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C	426.70	unknown	https://doi.org/10.1016/S0031-9422(00)85821-5 https://doi.org/10.1016/S0031-9422(00)86183-X
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(2R,3R,4S,5S,6R)-2-[[(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	163042754	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1016/S0031-9422(00)85821-5 https://doi.org/10.1016/S0031-9422(00)86183-X
(3R,5S,9S,10R,13S,14R,17S)-17-[(Z,2S,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	163185567	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1016/S0031-9422(00)86183-X https://doi.org/10.1016/S0031-9422(00)85821-5
(3S,5S,9S,10S,13R,14R,17R)-17-[(Z,2S,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	162958790	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1016/S0031-9422(00)85821-5 https://doi.org/10.1016/S0031-9422(00)82170-6
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	521229	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1016/S0031-9422(00)86183-X https://doi.org/10.1016/S0031-9422(00)82170-6 https://doi.org/10.1016/S0031-9422(00)85821-5
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	86821	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.3109/13880209409082993
24-Ethylcholest-5-en-3beta-ol	22012	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.3109/13880209409082993
beta-Sitosterol 3-O-beta-D-galactopyranoside	296119	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1016/S0031-9422(00)85821-5 https://doi.org/10.1016/S0031-9422(00)86183-X
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
1,2,3,4,5-Cyclohexanepentol	101715	Click to see C1C(C(C(C(C1O)O)O)O)O	164.16	unknown	https://doi.org/10.1016/S0031-9422(00)85821-5 https://doi.org/10.1016/S0031-9422(00)86183-X
> Organoheterocyclic compounds / Indoles and derivatives
10-Hydroxy-1'-methoxy-1-propanoylspiro[7-oxa-2-azatricyclo[4.3.1.03,9]decane-5,3'-indole]-2'-one	75051795	Click to see CCC(=O)C12C3COC(C1O)C4(CC3N2)C5=CC=CC=C5N(C4=O)OC	358.40	unknown	https://doi.org/10.1016/S0031-9422(00)85821-5 https://doi.org/10.1016/S0031-9422(00)82170-6
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin	5280343	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	302.23	unknown	https://doi.org/10.1016/S0031-9422(00)82170-6

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Manilkara hexandra

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top